ICON plc
ICON plc
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.

Senior Clinical Research Associate – Quebec Remote | ICON plc

Monitor cardiovascular and respiratory clinical trials across Quebec for ICON plc, supporting site compliance, data quality, and adherence to study protocols.

Description

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Lead monitoring work with an emphasis on quality and ongoing process improvement
  • Evaluate site compliance with protocols, regulations, and Good Clinical Practice requirements
  • Perform site visits to review performance, address issues, and support effective study delivery
  • Work with cross-functional teams to coordinate accurate, timely data collection and reporting
  • Train and advise site personnel and fellow Clinical Research Associates
  • Develop and sustain effective working relationships with site teams and study stakeholders
  • Monitor cardiovascular and respiratory studies conducted in Quebec

Requirements

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience, including a strong command of clinical trial processes and regulatory obligations
  • Demonstrated ability to oversee multiple sites and projects concurrently, with strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management, plus proficiency with applicable clinical trial systems and tools
  • Strong communication, interpersonal, and stakeholder-management capabilities, including the ability to promote compliance in a complex setting
  • Availability to travel as needed, approximately 60% of the time
  • Legal authorization to work in the country where the position is located

Benefits

  • Base salary with performance-based incentives
  • Health and wellness programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension programs
  • Life insurance and disability protection
  • Employee assistance programs and wellbeing support resources
  • Professional development through structured training and career progression pathways

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